?cone-rod dystrophy Gene Set

Dataset	OMIM Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	A retinal degeneration that is an inherited progressive disease that causes deterioration of the cone and rod photoreceptor cells and often results in blindness. (Human Disease Ontology, DOID_0050572)
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Genes

1 genes associated with the ?cone-rod dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol	Name
UNC119	unc-119 homolog (C. elegans)